CLAISEN REARRANGEMENT IN N-ALLYLANILINE SERIES

DOI: 10.1007/BF00953146

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 1149 - 1153 (1983)

Update date:2022-09-26

Topics:

Authors:

Abdarakhmanov, I. B.

Sharafutdinov, V. M.

Nigmatullin, N. G.

Mustafin, A. G.

Saraeva, Z. M.

Tolstikov, G. A.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1007/BF00953146

Full text of DOI:10.1007/BF00953146

Products guided by the article

Product name:(Z)-3-chloropenta-1,3-diene

Cas No:20476-54-4

R&D Labs maybe for 20476-54-4

Taizhou Green Peptide Trading Co., Ltd.

Contact:--15314709780

Address:Room 1501, No71, Yuehe Road, Taizhou City, Zhejiang Province, China
Zhengzhou Yuanli Biological Technology Co., Ltd.

Contact:+86-371-67897870/67897895

Address:No. 38, Qingyang Street, Zhengzhou, Henan, China
HAINAN JINYING IMPORT AND EXPORT CO. LTD

Contact:+86-898-32875423

Address:A SECTION 19TH FL, TIMES SQUARE, NO.2 GUO MAO AVENUE HAIKOU, HAINAN, P. R. OF CHINA
AURORA CHEMICAL CO., LTD

Contact:86-532-68629711 13780605697

Address:NO 220 YANAN 3 ROAD,(POST ADMINISTRATION BUILDING),QINGDAO,CHINA
Suzhou BEC Fine Chemicals Co., Ltd.

website:http://www.bek.com.cn

Contact:0512-68095917　 18913193865

Address:6, Jin Shan Road, Suzhou New District, 215011 China Suzhou Nations Pharmaceutical Innovation Center Inside

Relevant to this article

Use of a pharmacophore model for the design of EGFR tyrosine kinase inhibitors: Isoflavones and 3-phenyl-4(1H)-quinolones

Doi:10.1021/jm980551o
(1999)
Synthesis of new benzylic ethers of oximes derived from 1-phenyl- pyrazole compounds

Doi:10.1080/00397919808005973
(1998)
The alkyne pathway to keramadine from the marine sponge Agelas sp.

Doi:10.1016/S0040-4039(98)00341-4
(1998)
An axially chiral phosphine ligand based on restricted rotation in N-arylimides

Doi:10.1016/S0040-4039(01)01482-4
(2001)
Identification of a Novel Oxadiazole Inhibitor of Mammalian Target of Rapamycin

Doi:10.1002/bkcs.11965
(2020)
An efficient synthesis of a key intermediate of DU-6859a via asymmetric microbial reduction

Doi:10.1248/cpb.46.587
(1998)

Article Doi